FDA.reportPublic FDA data

DayClear Hand Sanitizer Gel

Manufacturer
GM Pharmaceuticals, INC
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:34:42

Label at a glance#

ProductDayClear Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

■ put enough product in your palm to cover all surfaces of both hands and rub hands together briskly until dry ■ children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Purpose

OTC - PURPOSE SECTION

Ethyl Alcohol 62% v/v...........................Antimicrobial

Use

INDICATIONS & USAGE SECTION

■ hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ put enough product in your palm to cover all surfaces of both hands and rub hands together briskly until dry

■ children under 6 years of age should be supervised when using this product

Other information

OTHER SAFETY INFORMATION

■ store at 20-30°C (68-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, carbomer, chamomilla recutita (matricaria) flower extract, diisopropylamine, glycerin, isopropyl myristate, water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 58809-225-02
DayClear
HAND
SANITIZER
GEL
2 FL OZ (59 mL)

PRINCIPAL DISPLAY PANEL NDC 58809-225-02 DayClear HAND SANITIZER GEL 2 FL OZ (59 mL)PRINCIPAL DISPLAY PANEL NDC 58809-225-02 DayClear HAND SANITIZER GEL 2 FL OZ (59 mL)

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 58809-225-08
DayClear
HAND
SANITIZER
GEL
8 FL OZ (237 mL)

PRINCIPAL DISPLAY PANEL NDC 58809-225-08 DayClear HAND SANITIZER GEL 8 FL OZ (237 mL)PRINCIPAL DISPLAY PANEL NDC 58809-225-08 DayClear HAND SANITIZER GEL 8 FL OZ (237 mL)

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 58809-225-32
DayClear
HAND
SANITIZER
GEL
32 FL OZ (946 mL)

PRINCIPAL DISPLAY PANEL NDC 58809-225-32 DayClear HAND SANITIZER GEL 32 FL OZ (946 mL)PRINCIPAL DISPLAY PANEL NDC 58809-225-32 DayClear HAND SANITIZER GEL 32 FL OZ (946 mL)

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 58809-225-12

DayClear

HAND

SANITIZER

GEL

12 fl. oz. (355 mL)

PDP 12ozPDP 12oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58809-225-022022-03-09C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-082022-03-09C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-122022-03-09C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-322022-03-09C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-022022-01-28C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-082022-01-28C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-122022-01-28C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel
58809-225-322022-01-28C16284748780-1d6a99b39-8a14-a426-e053-dadaa90af4c2DayClear Hand Sanitizer Gel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58809-22558809-225-02, 58809-225-08, 58809-225-32, 58809-225-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CHAMOMILEFGL3685T2XIACT
DIISOPROPYLAMINEBR9JLI40NOIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d9d42b0e-4f0c-f3d9-e053-2995a90ae65bc7a65406-3339-4c46-ab1a-72537ef482b72022-03-09WarningsExact identifier
spl set id: c7a65406-3339-4c46-ab1a-72537ef482b7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.